Canonical Allele Identifier: CA375564463
Community Standard Title: NM_019892.6(INPP5E):c.1073C>T (p.Pro358Leu)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136433241G>A , CM000671.2:g.136433241G>A GRCh38
NC_000009.11:g.139327693G>A , CM000671.1:g.139327693G>A GRCh37
NC_000009.10:g.138447514G>A NCBI36
NG_016126.1:g.11564C>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1073C>T MANE Select NP_063945.2:p.Pro358Leu
ENST00000371712.4:c.1073C>T MANE Select ENSP00000360777.3:p.Pro358Leu
NM_001318502.1:c.1073C>T NP_001305431.1:p.Pro358Leu
NM_001318502.2:c.1073C>T NP_001305431.1:p.Pro358Leu
NM_019892.4:c.1073C>T NP_063945.2:p.Pro358Leu
NM_019892.5:c.1073C>T NP_063945.2:p.Pro358Leu
ENST00000371712.3:c.1073C>T ENSP00000360777.3:p.Pro358Leu
ENST00000676019.1:c.1035-64C>T ENSP00000501984.1:n.1035-64C>T
XM_005266094.2:c.1073C>T XP_005266151.1:p.Pro358Leu
XM_017014926.1:c.1073C>T XP_016870415.1:p.Pro358Leu
XR_929828.1:n.1513C>T
XR_929828.2:n.1515C>T